Coquillat G - Search Results

1

[Febrile dysarthria revealing myxoma of the left atrium. Neuroradiological aspects].

Taillandier L, Anxionnat R, Hoen B, Godet E, Roux PM, Coquillat G. Taillandier L, et al. Among authors: coquillat g. Presse Med. 1993 May 29;22(19):919-20. Presse Med. 1993. PMID: 8378284 French. No abstract available.

2

Post-myelography meningoencephalitis caused by Streptococcus agalactiae.

Hoen B, Taillandier L, Coquillat G. Hoen B, et al. Among authors: coquillat g. J Infect. 1993 May;26(3):337-9. doi: 10.1016/0163-4453(93)95899-t. J Infect. 1993. PMID: 8505574 No abstract available.

3

Lafora disease is not linked to the Unverricht-Lundborg locus.

Labauge P, Beck C, Bellet H, Coquillat G, Vespignani H, Dulac O, Gilgenkrantz S, Dravet C, Genton P, Pellissier JF, et al. Labauge P, et al. Among authors: coquillat g. Am J Med Genet. 1995 Feb 27;60(1):80-4. doi: 10.1002/ajmg.1320600114. Am J Med Genet. 1995. PMID: 7485240

4

Peripheral neuropathy following fetal bovine cell rabies vaccine.

Courrier A, Stenbach G, Simonnet P, Rumilly P, Lopez D, Coquillat G, Scherer C, Chopin J. Courrier A, et al. Among authors: coquillat g. Lancet. 1986 May 31;1(8492):1273. doi: 10.1016/s0140-6736(86)91410-8. Lancet. 1986. PMID: 2872413 No abstract available.

5

[Anomalies in fatty acids distribution and superoxide dismutase activity in lymphocytes of an adult with atypical ceroid lipofuscinosis].

Rumbach L, Warter JM, Coquillat G, Marescaux C, Collard M, Rohmer F, Bieth R, Zawislak R. Rumbach L, et al. Among authors: coquillat g. Rev Neurol (Paris). 1983;139(4):269-76. Rev Neurol (Paris). 1983. PMID: 6310717 French.

6

Stuporous episodes during treatment with sodium valproate: report of seven cases.

Marescaux C, Warter JM, Micheletti G, Rumbach L, Coquillat G, Kurtz D. Marescaux C, et al. Among authors: coquillat g. Epilepsia. 1982 Jun;23(3):297-305. doi: 10.1111/j.1528-1157.1982.tb06195.x. Epilepsia. 1982. PMID: 6806087

7

[Atypical ceroid-lipofuscinosis in the adult or atypical spinocerebellar degeneration with intracytoplasmic inclusions? (author's transl)].

Rumbach L, Coquillat G, Simony N, Marescaux C, Walter P. Rumbach L, et al. Among authors: coquillat g. Rev Otoneuroophtalmol. 1981 Mar-Apr;53(2):111-20. Rev Otoneuroophtalmol. 1981. PMID: 6270769 French. No abstract available.

8

Treatment of Huntington disease with gamma-acetylenic GABA an irreversible inhibitor of GABA-transaminase: increased CSF GABA and homocarnosine without clinical amelioration.

Tell G, Böhlen P, Schechter PJ, Koch-Weser J, Agid Y, Bonnet AM, Coquillat G, Chazot G, Fischer C. Tell G, et al. Among authors: coquillat g. Neurology. 1981 Feb;31(2):207-11. doi: 10.1212/wnl.31.2.207. Neurology. 1981. PMID: 6258106 Clinical Trial.

9

[An autosomal recessive syndrome with myopathy and central and peripheral nervous system involvement (author's transl)].

Warter JM, Marescaux C, Coquillat G, Walter P, Micheletti G, Rohmer F. Warter JM, et al. Among authors: coquillat g. J Neurol Sci. 1981 Jan;49(1):135-51. doi: 10.1016/0022-510x(81)90195-7. J Neurol Sci. 1981. PMID: 6451671 French.

10

[The convulsive disease state. Apropos of 79 cases].

Mantz IM, Kopferschitt I, Tempe ID, Jaeger A, Micheletti G, Coquillat G. Mantz IM, et al. Among authors: coquillat g. Minerva Med. 1980 Oct 20;71(40):2883-8. Minerva Med. 1980. PMID: 7454074 Italian. No abstract available.

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